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17152-81-7

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17152-81-7 Usage

General Description

Phenol, 4-(1,7,7-trimethylbicyclo[2.2.1]hept-2-yl)-, is a chemical compound with the molecular formula C15H22O. It is a derivative of phenol with a bicyclic structure, containing a seven-membered ring. This chemical is commonly used as a fragrance and flavor ingredient in various cosmetic and personal care products. It is known for its aromatic and minty odor, and is often used in perfumes, soaps, and lotions. Additionally, it has antimicrobial properties, making it useful in certain topical antiseptic formulations. Phenol,4-(1,7,7-trimethylbicyclo[2.2.1]hept-2-yl)- may also have potential applications in the pharmaceutical and medical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 17152-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,5 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17152-81:
(7*1)+(6*7)+(5*1)+(4*5)+(3*2)+(2*8)+(1*1)=97
97 % 10 = 7
So 17152-81-7 is a valid CAS Registry Number.

17152-81-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl)phenol

1.2 Other means of identification

Product number -
Other names 4-Isobornyl-phenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17152-81-7 SDS

17152-81-7Downstream Products

17152-81-7Relevant articles and documents

Alkylation of phenol by β-pinene in the presence of aluminum phenolate

Chukicheva,Shumova,Kuchin

experimental part, p. 43 - 46 (2012/07/17)

The alkylation of phenol by β-pinene using Al(OPh)3 as a catalyst was studied. It was found that the composition of the products depended on the ratio of starting materials. The principal products were chromane-type ethers with an equimolar ratio of starting materials and an excess of phenol. ortho-Alkylated phenol and an ether with a terpene substituent of bornyl structure were formed with a two-fold excess of β-pinene.

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